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1008364-25-7

(C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-)) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1008364-25-7 Structure

  • Basic information

    1. Product Name: (C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-))
    2. Synonyms: (C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-))
    3. CAS NO:1008364-25-7
    4. Molecular Formula:
    5. Molecular Weight: 690.872
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1008364-25-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-))(CAS DataBase Reference)
    10. NIST Chemistry Reference: (C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-))(1008364-25-7)
    11. EPA Substance Registry System: (C5Me5)Ir(2-(2-trifluoromethylanilino-4,6-di-tert-butylphenol(2-))(1008364-25-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1008364-25-7(Hazardous Substances Data)

1008364-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1008364-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,3,6 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1008364-25:
(9*1)+(8*0)+(7*0)+(6*8)+(5*3)+(4*6)+(3*4)+(2*2)+(1*5)=117
117 % 10 = 7
So 1008364-25-7 is a valid CAS Registry Number.

1008364-25-7Downstream Products

1008364-25-7Relevant articles and documents

Redox-switched oxidation of dihydrogen using a non-innocent ligand

Ringenberg, Mark R.,Kokatam, Swarna Latha,Heiden, Zachariah M.,Rauchfuss, Thomas B.

, p. 788 - 789 (2008)

Organometallic complexes containing non-innocent ligands of the type Cp*Ir(tBAFPh)(1), where H2tBAFPh is 2-(2-trifluoromethyl)anilino-4,6-di-tert-butylphenol, were found to activate H2 in a redox-switchable manner. The 16e- complex 1 was inert with respect to H2, CO, as well as conventional basic substrates until oxidation. Oxidation of 16-electron 1 with 1 equiv of Ag+ resulted in ligand-centered oxidation affording salts of [1]+, which were characterized by crystallographically, EPR, and elemental analyses. [1]+ was reduced to 1 in the presence of H2 and the sterically hindered base, 2,6-(tBu)2C5H3N, via a pathway that is first-order in both metal and dihydrogen. Compound [1]+ forms adducts with MeCN, which inhibits catalysis. The catalytic oxidation of H2 was established by electrochemical methods to be associated with the monocation. Copyright

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